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Clinical Trials in Egypt / NCT07238985
Recruiting Phase 1/2

Cilostazol in the Treatment of Nonalcoholic Fatty Liver Disease

NCT07238985 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 1/2
Started
2025-11-01
Last updated
2025-11-25

Condition(s) studied

Fatty Liver

Investigational drug(s) / intervention(s)

Standard therapyCilostazol →

Standard therapy: • The standard conventional therapy in both groups included regular exercise in the form of any physical activity as walking, cycling, etc. for 30-45 minutes minimum 5 days per week in addition to calorie restriction in overweight and obese patients (1200-1500 and 1000-1200 kcal/day for men and women, respectively).

Cilostazol: Cilostazol is a 2-hydroxyquinolone derivative and a drug approved for improving the claudication distance. Other studies have shown that Cilostazol can ameliorate hepatic steatosis, but the specific mechanism is still unknown

Study summary

Nonalcoholic fatty liver disease (NAFLD) is a global public health concern, and the leading cause of chronic liver disease, especially in developed countries (1). NAFLD is characterized by lipid accumulation in the liver not attributed to other causes. NAFLD is characterized by excessive hepatic fat accumulation without other recognized causes of increased fat content (e.g., alcohol, virus, drugs, and autoimmunity). According to the Clinical Practice Guidelines of the European Association for the Study of the Liver, the diagnosis of NAFLD requires the exclusion of daily alcohol consumption \>30 g for men and \>20 g for women

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: Either male or female adult patients (\>18 years) with fatty liver diagnosis by using upper abdominal ultrasound echography (US). Exclusion Criteria: Pregnant and/or lactating women, excessive alcohol use (defined as an average alcohol intake \> 30 g per day in men and \> 20 g per day in women). Other etiology of chronic liver diseases such as viral hepatitis, drug-induced hepatitis, autoimmune hepatitis. Patients suffering from chronic kidney disease, hyper/hypoparathyroidism, and congestive heart failure patients

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Mostafa Bahaa Damietta New Damietta Recruiting

More Tanta University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07238985 on ClinicalTrials.gov ↗ ← All trials in Egypt